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rs2067051

From SNPedia

Orientationminus
Stabilizedminus
Make rs2067051(A;A)
Make rs2067051(A;G)
Make rs2067051(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position1996938
GeneH19, MIR675
is asnp
is mentioned by
dbSNPrs2067051
ebirs2067051
HLIrs2067051
Exacrs2067051
Varsomers2067051
Maprs2067051
PheGenIrs2067051
hapmaprs2067051
1000 genomesrs2067051
hgdprs2067051
ensemblrs2067051
gopubmedrs2067051
geneviewrs2067051
scholarrs2067051
googlers2067051
pharmgkbrs2067051
gwascentralrs2067051
openSNPrs2067051
23andMers2067051
23andMe allrs2067051
SNP Nexus

SNPshotrs2067051
SNPdbers2067051
MSV3drs2067051
GWAS Ctlgrs2067051
GMAF0.3448
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20639793OA-icon.png] Association of birth weight with polymorphisms in the IGF2, H19, and IGF2R genes

[PMID 15885138OA-icon.png] Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.

[PMID 16839189OA-icon.png] Human imprinted chromosomal regions are historical hot-spots of recombination.


GET Evidence
H19-V94I
aa_change Val94Ile
aa_change_short V94I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.361111
summary